| Posted: 18 August 2005 at 9:50pm | IP Logged
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I would definetely like to help in any way possible, i didnt know anything about SPD before my 2nd pg, but suspect i had it with my 1st pg but my naff docs in london didnt know anything about the condition or failed to correctly diagnose me. luckily for me since moving to kings lynn my gp is fab and has been excellent b4 and after pg.
i know just how serious the condition can be, my cousin got the worst kind of spd, she had the diastisis(sp) version where her symphisis pubis completely tore and so she ended up bed ridden for 6 months of her 2nd pg and couldnt look after her 2 yr old dd. and has since had an op to repair the damage, she has been advised that her pelvis is now likely to be too weak to carry any more babies.
i agree far more women should be informed of this and even told about it at the beginning of pg, to help look for the symptoms early on and hopefully prevent too much damage being done.
as you can see i feel very strongly on this, mainly as i am still having some problems over 4 months later, i rolled over in bed the other night and ended up in agony for a few days as a result, my gp has said can take upto 6 months to recover, so i am hoping it settles again soon.
any help i can be please let me know i am more than willing to help.
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